Who We Are
The WSA is the most comprehensive resource for people and families living with Williams syndrome, as well as doctors, researchers, and educators.
What We Do
The WSA provides resources, support, and the latest medical information to help individuals with WS today and throughout their lives. We are dedicated to improving the lives of people living with Williams syndrome. We are organizing a convention in Buffalo, NY, in July 2026. During the convention, we provide informational/educational sessions for parents/caregivers, while individuals with WS of all ages participate in programming with the help of volunteers.
Details
| (630) 732-1515 ext. 6307321515 | |
| kboxall@williams-syndrome.org | |
| Kristin Boxall | |
| Volunteer Coordinator | |
| https://www.williams-syndrome.org/convention-volunteers |
